How does the law regulate the manufacture of counterfeit drugs?
In Hawaii, the manufacture of counterfeit drugs is regulated under a number of laws. Firstly, the Hawaii Revised Statutes (HRS) Chapter 486-F specifically prohibits the manufacture and distribution of counterfeit drugs. If any person is found to be knowingly making, manufacturing or selling counterfeit drugs, they can be fined and imprisoned. Hawaii is also one of several states that enacted the Drug Quality & Security Act (DQSA). Under the DQSA, any person who knowingly manufactures, distributes, sells, dispenses, or otherwise transfers counterfeit drugs, or a counterfeit device, is guilty of a felony and can be fined or imprisoned. The FDA also has the authority to investigate and prosecute counterfeit drug manufacturers under the Federal Food, Drug and Cosmetic Act (FD&C). If an individual is found to be manufacturing a counterfeit drug, the FDA may impose an injunction, a fine, or both. The FDA will also work with local and federal law enforcement to investigate and bring charges against counterfeit drug manufacturers. Lastly, the Controlled Substances Act (CSA) prohibits the manufacture and distribution of any controlled drugs, including counterfeit drugs. The penalties for violating this act depend upon the amount of the drug, the use of the drug, and the intent of the defendant. In short, Hawaii, like other states, is committed to stopping the manufacture of counterfeit drugs and has a number of laws in place to do so. People who are found to be engaged in this illegal behavior can be fined, imprisoned, and have their assets seized.
Related FAQs
What are the legal implications of drug patent infringement?What is the legal framework governing the sale of prescription drugs?
What is the legal definition of a prescription drug?
What are the implications of generic drug approval for brand name manufacturers?
What are the regulations governing the approval of generic drugs?
What is the impact of intellectual property rights in the pharmaceutical industry?
What is the role of the FDA in the regulation of pharmaceuticals?
What is the law regarding the use of personal data in the pharmaceutical industry?
What is the role of the FDA in the approval of drugs?
What are the legal requirements for conducting clinical trials?
Related Blog Posts
Navigating the Complexities of Pharmaceutical Laws - July 31, 2023The Basics of Pharmaceutical Law Regulations - August 7, 2023
Understanding the Role of the Food and Drug Administration in Pharmaceutical Law - August 14, 2023
Ensuring Compliance with Pharmaceutical Laws - August 21, 2023
Recognizing Key Elements of Pharmaceutical Law - August 28, 2023